Pt-on-Pd Dendritic Nanosheets with Enhanced Bifunctional Fuel Cell Catalytic Performance
Source abstract
Abstract
Pd-Pt bimetallic nanocrystals have become appealing in the electrocatalytic field by virtue of their synergy effects derived from the electronic coupling between two metals. Herein, a facile seed-mediated growth approach is reported for synthesis of Pt-on-Pd dendritic nanosheets (DNSs) through the growth of Pt branches on ultrathin Pd nanosheets (NSs). The as-obtained Pt-on-Pd DNSs exhibit superior catalytic activity toward both oxygen reduction reaction (ORR) and methanol oxidation reaction (MOR), with mass activities (MAs) 2.2 times higher for ORR and 3.4 times higher for MOR than commercial Pt/C catalysts. Moreover, these spatially separated Pt branches supported on 2D NSs also endow the Pt-on-Pd DNSs with impressive durability for ORR with only 18.9% loss in MA, whereas the Pt/C catalyst loses 50.0% after 10,000-cycle accelerated durability tests. This 2D DNS architecture can be extended to other 2D metallic NS substrates for constructing Pt-based electrocatalysts with excellent electrocatalytic performance.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Machine Learning in Materials Science
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Environmental Science, Shanxi University, Taiyuan, Shanxi 030006, PR China
Department of Materials Science and Engineering, College of Engineering, Peking University, Beijing 100871, PR China
Funding
National Natural Science Foundation of China · Young Sanjin Scholar Foundation of Shanxi Province · Program for the Young Talents of Higher Education Institution of Shanxi · Key R&D Project of Shanxi
References (43)
Show source-provided references
1. 10.1021/acs.chemrev.6b0029910.1021/acs.chemrev.6b00299 ↗
2. 10.1021/cr300096b10.1021/cr300096b ↗
3. 10.1021/ja111690g10.1021/ja111690g ↗
4. 10.1002/anie.20050438610.1002/anie.200504386 ↗
5. 10.1002/anie.20100586810.1002/anie.201005868 ↗
6. 10.1021/ja500590n10.1021/ja500590n ↗
7. 10.1021/acs.nanolett.5b0305710.1021/acs.nanolett.5b03057 ↗
8. 10.1021/nl401881z10.1021/nl401881z ↗
9. 10.1039/c2cs35173k10.1039/c2cs35173k ↗
10. 10.1038/nmat184010.1038/nmat1840 ↗
11. 10.1002/anie.20100428710.1002/anie.201004287 ↗
12. 10.1021/cr030063a10.1021/cr030063a ↗
13. 10.1021/jp100835b10.1021/jp100835b ↗
14. 10.1039/c0cp02167a10.1039/c0cp02167a ↗
15. 10.1039/c3ta13155f10.1039/c3ta13155f ↗
16. 10.1021/ja902256a10.1021/ja902256a ↗
17. 10.1021/ja202655j10.1021/ja202655j ↗
18. 10.1039/c3ta13954a10.1039/c3ta13954a ↗
19. 10.1016/j.electacta.2015.12.06810.1016/j.electacta.2015.12.068 ↗
20. 10.1021/ja111130t10.1021/ja111130t ↗
21. 10.1021/jacs.5b1005910.1021/jacs.5b10059 ↗
22. 10.1039/c6ce00816j10.1039/c6ce00816j ↗
23. 10.1002/smll.20160342310.1002/smll.201603423 ↗
24. 10.1021/acs.chemrev.6b0021110.1021/acs.chemrev.6b00211 ↗
25. 10.1021/nn901448310.1021/nn9014483 ↗
26. 10.1126/science.117037710.1126/science.1170377 ↗
27. 10.1039/c3cp52252k10.1039/c3cp52252k ↗
28. 10.1073/pnas.122210911010.1073/pnas.1222109110 ↗
29. 10.1039/b922148d10.1039/b922148d ↗
30. 10.1002/adma.20160482910.1002/adma.201604829 ↗
31. 10.1039/c4ce02062f10.1039/c4ce02062f ↗
32. 10.1021/ja801566d10.1021/ja801566d ↗
33. 10.1021/jacs.5b0464110.1021/jacs.5b04641 ↗
34. 10.1021/ja408645b10.1021/ja408645b ↗
35. 10.1002/anie.20110706110.1002/anie.201107061 ↗
36. 10.1039/c5nr07681a10.1039/c5nr07681a ↗
37. 10.1002/ange.20160473110.1002/ange.201604731 ↗
38. 10.1021/nn506387w10.1021/nn506387w ↗
39. 10.1149/1.183764610.1149/1.1837646 ↗
40. 10.1126/science.113594110.1126/science.1135941 ↗
41. 10.1002/advs.20160048610.1002/advs.201600486 ↗
42. 10.1039/c2jm15426a10.1039/c2jm15426a ↗
43. 10.1039/c7cc08346g10.1039/c7cc08346g ↗